ID   GM02036
AC   CVCL_7348
SY   GM2036; GM 02036; GM-02036; GM-2036; GM02036A; GMO2036A; C2036
DR   CLO; CLO_0032573
DR   BioSample; SAMN00807414
DR   BioSample; SAMN03253067
DR   Coriell; GM02036
DR   Wikidata; Q54837255
RX   CelloPub=CLPUB00387;
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=17668376;
RX   PubMed=29125828;
RX   PubMed=33038742;
CC   Population: Caucasian.
CC   Omics: Deep RNAseq analysis.
CC   Derived from sampling site: Skin. Cell type=Fibroblast.
OX   NCBI_TaxID=9606; ! Homo sapiens
SX   Female
AG   11Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 17-03-22; Version: 16
//
RX   CelloPub=CLPUB00387;
RA   Coriell L.L., Greene A.E., Mulivor R.A.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 7th edition. October 1980.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda (1980).
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//
RX   DOI=10.5962/bhl.title.4090;
RA   Coriell L.L., Greene A.E.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 4th edition. October 1977.";
RL   (In) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977).
//
RX   PubMed=17668376; DOI=10.1086/519248;
RA   Prandini P., Deutsch S., Lyle R., Gagnebin M., Delucinge-Vivier C.,
RA   Delorenzi M., Gehrig C., Descombes P., Sherman S.L.,
RA   Dagna-Bricarelli F., Baldo C., Novelli A., Dallapiccola B.,
RA   Antonarakis S.E.;
RT   "Natural gene-expression variation in Down syndrome modulates the
RT   outcome of gene-dosage imbalance.";
RL   Am. J. Hum. Genet. 81:252-263(2007).
//
RX   PubMed=29125828; DOI=10.1242/dmm.030536;
RA   Napierala J.S., Li Y.-J., Lu Y., Lin K., Hauser L.A., Lynch D.R.,
RA   Napierala M.;
RT   "Comprehensive analysis of gene expression patterns in Friedreich's
RT   ataxia fibroblasts by RNA sequencing reveals altered levels of protein
RT   synthesis factors and solute carriers.";
RL   Dis. Model. Mech. 10:1353-1369(2017).
//
RX   PubMed=33038742; DOI=10.1016/j.scr.2020.102011;
RA   Xu X.-G., Pradhan M., Xu M., Cheng Y.-S., Beers J.K., Linask K.L.,
RA   Lin Y.-S., Zheng W., Zou J.-H.;
RT   "Four induced pluripotent stem cell lines (TRNDi021-C, TRNDi023-D,
RT   TRNDi024-D and TRNDi025-A) generated from fibroblasts of four healthy
RT   individuals.";
RL   Stem Cell Res. 49:102011-102011(2020).
//